The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127553471 12755347 1 I 20160909 20160916 20160916 EXP JP-ASTRAZENECA-2016SE96092 ASTRAZENECA 90.00 YR F Y 0.00000 20160916 PH JP JP

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127553471 12755347 1 PS FASLODEX FULVESTRANT 1 Intramuscular U 21344 INJECTION
127553471 12755347 2 SS AROMASIN EXEMESTANE 1 Oral 25.0MG UNKNOWN U U 0 25 MG TABLET
127553471 12755347 3 SS AROMASIN EXEMESTANE 1 Oral 25.0MG UNKNOWN U U 0 25 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127553471 12755347 1 Breast cancer
127553471 12755347 2 Breast cancer
127553471 12755347 3 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
127553471 12755347 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127553471 12755347 Bone density decreased
127553471 12755347 Fall
127553471 12755347 Fracture

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127553471 12755347 1 2016 0
127553471 12755347 3 2016 0